Job Description

You will work closely with all members of the Research Delivery Team, performing all aspects of administrative duties related to clinical trial delivery.

You will work according to Good Clinical Practice (GCP), standard operating procedures (SOPs) and trust policies.

Main duties

We are looking for a motivated and effective clinical trials administrator with a ‘can do’ attitude and an eye for detail. You should be organized, able to demonstrate initiative and be able to priorities effectively.

This will be a rewarding post, adding value to the working practices of this nationally recognized team who offer research opportunities to patients with complex medical conditions.

Required Knowledge, Skills, and Abilities

• Knowledge and relevant experience equivalent to NVQ Level 3
• ECDL or equivalent
• First level degree
• IT literate, including ability to demonstrate Microsoft Office and internet skills, with an aptitude for developing IT systems to record and retrieve clinical trials data
• Effective communication and interpersonal skills
• Ability to manage and priorities own workload with minimal supervision and to strict timescales
• Data entry experience with methodical approach and attention to detail
• Good comprehension skills
• Set up and manage documentation systems
• Ability to pick up new ideas quickly
• Displays sensitivity to others and respects confidentiality
• Understanding of data protection and Caldicott Guidelines
• Experience of working autonomously and as part of a Team.
• General administration experience
• Maintain professional development
• Positive, enthusiastic and committed
• Supportive to colleagues
• Confident and self-motivated
• Demonstrates flexibility in working hours, ability to move between sites
• Experience of working in a clinical environment.
• Relevant experience of research.
• Some knowledge of the healthcare environment